AutismKB 2.0

Annotation Detail for C22orf25


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Basic Information Top
Gene Symbol:C22orf25 ( DKFZp761P1121 )
Gene Full Name: chromosome 22 open reading frame 25
Band: 22q11.21
Quick LinksEntrez ID:128989; OMIM: NA; Uniprot ID:CV025_HUMAN; ENSEMBL ID: ENSG00000183597; HGNC ID:
Relate to Another Database: SFARIGene; denovo-db
Post Translation Modification Top
No data
No data
Location(AA) Modification Resource
98O-linkedHMM predict
116Phosphotyrosine(Abl)HMM predict
162Phosphothreonine(CDC2)HMM predict
216Phosphotyrosine(Abl)HMM predict
216Phosphotyrosine(Jak)HMM predict
Validated transcription factor binding site by ChIP-Chip and ChIP-Seq
  • RefSeq ID: NM_152906
  • Location:chr22 18388630-18433446
  • strand:+
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF G2GSE9613 18388431 18388719 288 56
NFkBII GM12892GSE19485 18387792 18389287 1495 91
PHF8 HeLaGSE20725 18387789 18389314 1525 79
hScc1 BcellGSE12603 18388250 18388888 638 62
p130 QuiescentGSE19898 18388201 18388453 252 304
p130 shRbQuiescentGSE19898 18387691 18388468 777 551
No data
Transcrip Factors Experimental Cell Database TF Binding Start TF Binding End TF Binding Length The Distance to Gene
CTCF CD4GSE12889 18428535 18428676 141 0
CTCF CD4SISSRdata 18428535 18428676 141 0
CTCF G2GSE9613 18419686 18420324 638 0
Gata1 K562GSE18868 18392674 18393700 1026 0
Gata2 K562GSE18868 18391678 18395250 3572 0
TFAP2C MCF7GSE21234 18394035 18394511 476 0
TFAP2C MCF7GSE21234 18429933 18430593 660 0
hScc1 BcellGSE12603 18425357 18425528 171 0
p130 shRbQuiescentGSE19898 18389007 18389838 831 0
Validated miRNA targets Top
Cis-Nats regulation Top
Cluster ID Plue Type Plus Gene Name Plus Chromosome Plus Start Plus End Overlap Length Minus Type Minus Gene Name Minus Chromosome Minus Star Minus End Type
17150 mRNA DKFZp761P1121 chr22 18383184 18428001 583 EST chr22 18426628 18427782Sense/Antisense (SA) pairs

Simple Query:


  (e.g. CHD8)

Syndromic Genes

Non-syndromic Genes

AutismKB Statistics

  • Studies: 1,036
  • Genes: 1,379
  • CNVs/SVs: 5,420
  • SNVs/Indels: 11,669
  • de novo Mutations: 5,669
  • Mosaics: 789
  • Linkage Regions: 172
  • Paper Collected: 6/30/2018
  • Last Update: 8/26/2018